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Exploring the Optimal Duration of a Group-based Online Behavioral Weight Loss Program

2020年11月12日 更新者:Jean R. Harvey, PhD, RD、University of Vermont
This online pilot weight loss study will explore the feasibility of recruiting individuals to an established online behavioral weight loss program of varying duration (4 months vs. 6 months), We will compare 6-month weight losses between the two programs of shorter and longer duration, respectively, and obtain data to characterize weight maintenance experiences and retention. Both groups will receive the same intervention; the only difference is the number of weeks the group will meet. Both groups will complete follow ups at 2, 4, 6, and 12 months (12 months after the study begins).

研究概览

详细说明

Obesity presents a vexing public health challenge. Effective behavioral weight control treatments are available, loss, and projections show these interventions could have a significant impact on overall population health if the interventions were more broadly available. Internet delivery of behavioral lifestyle interventions has potential for broad reach and is thus an attractive option, although average weight losses tend to be lower than in a comparable behavioral program delivered in-person. Nonetheless, internet-delivered group behavioral weight control programs which incorporate synchronous chat "group sessions" can produce an average of 5% weight loss, with almost a quarter of participants losing at least 10% of their body weight at 6-months, and thus offer weight losses which are clinically significant. Online programs are more cost effective than in-person delivery of the same program, but efforts to optimize the delivery of online programs to achieve the best weight outcomes balanced against delivery cost are in their infancy. The current feasibility study seeks to explore critical elements to allow testing of whether a moderate dose program (16 online weekly video chat sessions) can produce weight losses comparable to the higher dose (24 weekly video chat sessions) internet-delivered behavioral weight loss program which is the established standard which we have demonstrated effective in the past. This pilot study will provide proof-of-concept to determine whether the approach is promising and if it is feasible to conduct. The pilot will explore the feasibility of recruiting individuals to weight loss programs of varying duration (4 months vs. 6 months), refine our ability to deliver the 16-session program, compare 6-month weight losses between the two programs of shorter and longer duration, respectively, and obtain data to characterize weight maintenance experiences and retention over the 12-month study period.

Up to 80 individuals will be randomized into an online behavioral weight loss program lasting 4 months or 6 months. Individuals will meet weekly for one hour in a synchronous chat session with an experienced behavioral weight control counselor. Participants will be followed over 12 months from study start.

研究类型

介入性

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • South Carolina
      • Columbia、South Carolina、美国、29208
        • University of South Carolina
    • Vermont
      • Burlington、Vermont、美国、05405
        • Behavioral Weight Management Program/Univ of Vermont

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

是的

有资格学习的性别

女性

描述

Inclusion Criteria:

  • female
  • BMI between 25-55
  • free of medical problems that might contraindicate participation in a behavioral weight reduction program containing an exercise component
  • not currently on medication that might affect weight loss
  • not currently pregnant or pregnant in the previous 6 months or currently breastfeeding
  • not enrolled in another weight reduction program
  • must have a computer (at home or work) with access to the Internet and a video camera
  • must have a smart phone (to allow use of step counting and dietary intake self-monitoring apps)
  • Only one member of a household will be eligible to participate
  • must successfully complete a self-monitoring diary of foods consumed for a week during screening for study eligibility
  • demonstrate the ability to access the website successfully (practice chat)
  • agree to be randomized to either group
  • must be willing to share access to self-monitoring information collected via the app MyFitnessPal, and Fitbit.com weight data collected via the digital smart scale (scale will be provided)

Exclusion Criteria:

  • have had a heart attack or a stroke in the past 6 months,
  • have ever had weight loss surgery,
  • have lost more than 10 pounds in the previous 6 months,
  • are currently taking medications for weight loss,
  • are required by their doctor to follow a special diet (other than a low fat diet)
  • have plans to move from the area in the upcoming 12 months
  • who have schedules that will make it likely that they will have difficulty attending the scheduled "chat" groups

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Four Month Duration
Participants will meet weekly online via video chat with an experienced behavioral weight loss counselor in a synchronous 1-hour chat session for 16 weeks in a well-established behavioral weight loss program.
Participants meet weekly on line with other group participants for 16 weeks. The group-based online behavioral weight control program incorporates the elements of current thinking and empirical data on successful weight loss programs, including restricted calorie intake and increased physical activity. Key behavioral strategies to facilitate making sustained changes in dietary habits and activity patterns are introduced, promoted, and reinforced throughout the program. Weekly "group meetings" in a video chat forum led by an experienced group weight control counselor are the venue for the group process, and extensive web-based resources to support behavior changes are offered. The online groups are "closed" such that those individuals who start the group remain in that group for the duration of their participation. Weight loss counselor will provide feedback and encouragement to participants after reviewing food diaries via weekly emails.
有源比较器:Six Month Duration
Participants will meet weekly online via video chat with an experienced behavioral weight loss counselor in a synchronous 1-hour chat session for 24 weeks in a well-established behavioral weight loss program.
Participants meet weekly on line with other group participants for 24 weeks. The group-based online behavioral weight control program incorporates the elements of current thinking and empirical data on successful weight loss programs, including restricted calorie intake and increased physical activity. Key behavioral strategies to facilitate making sustained changes in dietary habits and activity patterns are introduced, promoted, and reinforced throughout the program. Weekly "group meetings" in a video chat forum led by an experienced group weight control counselor are the venue for the group process, and extensive web-based resources to support behavior changes are offered. The online groups are "closed" such that those individuals who start the group remain in that group for the duration of their participation. Weight loss counselor will provide feedback and encouragement to participants after reviewing food diaries via weekly emails.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Change in Weight from baseline to 2, 4, 6 and 12 months
大体时间:2 months, 4 months, 6 months, 12 months
Weight loss at each follow-up will be calculated as % kg lost from baseline.
2 months, 4 months, 6 months, 12 months

次要结果测量

结果测量
措施说明
大体时间
Process measures: Attendance by subjects at weekly online meetings
大体时间:2,4,6 months
The group facilitator will take attendance at weekly online class meetings. Attendance at on-line meetings will be calculated as % of meetings actually attended out of 16 or 24 meetings that were scheduled according to condition assignment
2,4,6 months
Process measures: Completion of weekly online treatment modules by subjects
大体时间:2, 4, 6 months
Completion of online treatment modules by each subject by condition will be calculated as % modules completed out of 16 or 24 modules scheduled according to condition assignment. Module completion is defined as viewing the module and completing the online activity questions associated with each respective module.
2, 4, 6 months

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Delia Smith West, PhD、University of South Carolina
  • 首席研究员:Jean R Harvey, PhD、University of Vermont

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (预期的)

2020年7月1日

初级完成 (预期的)

2021年1月1日

研究完成 (预期的)

2021年2月1日

研究注册日期

首次提交

2020年11月2日

首先提交符合 QC 标准的

2020年11月12日

首次发布 (实际的)

2020年11月13日

研究记录更新

最后更新发布 (实际的)

2020年11月13日

上次提交的符合 QC 标准的更新

2020年11月12日

最后验证

2020年11月1日

更多信息

与本研究相关的术语

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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